JP2016511273A - D−グルシトール,1−デオキシ−1−(メチルアミノ)−,1−(6−アミノ−3,5−ジフルオロピリジン−2−イル)−8−クロロ−6−フルオロ−1,4−ジヒドロ−7−(3−ヒドロキシアゼチジン−1−イル)−4−オキソ−3−キノリンカルボン酸塩の結晶型 - Google Patents
D−グルシトール,1−デオキシ−1−(メチルアミノ)−,1−(6−アミノ−3,5−ジフルオロピリジン−2−イル)−8−クロロ−6−フルオロ−1,4−ジヒドロ−7−(3−ヒドロキシアゼチジン−1−イル)−4−オキソ−3−キノリンカルボン酸塩の結晶型 Download PDFInfo
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- JP2016511273A JP2016511273A JP2015561727A JP2015561727A JP2016511273A JP 2016511273 A JP2016511273 A JP 2016511273A JP 2015561727 A JP2015561727 A JP 2015561727A JP 2015561727 A JP2015561727 A JP 2015561727A JP 2016511273 A JP2016511273 A JP 2016511273A
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- hydroxyazetidin
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- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
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- 239000000314 lubricant Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
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- 229940095102 methyl benzoate Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 229960003085 meticillin Drugs 0.000 description 1
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- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical group 0.000 description 1
- FABPRXSRWADJSP-MEDUHNTESA-N moxifloxacin Chemical compound COC1=C(N2C[C@H]3NCCC[C@H]3C2)C(F)=CC(C(C(C(O)=O)=C2)=O)=C1N2C1CC1 FABPRXSRWADJSP-MEDUHNTESA-N 0.000 description 1
- 229960003702 moxifloxacin Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
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- 239000006186 oral dosage form Substances 0.000 description 1
- 229940126701 oral medication Drugs 0.000 description 1
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- 230000000737 periodic effect Effects 0.000 description 1
- 206010034674 peritonitis Diseases 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 description 1
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
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- 239000003380 propellant Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002105 relative biological effectiveness Effects 0.000 description 1
- 208000020029 respiratory tract infectious disease Diseases 0.000 description 1
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- 239000012488 sample solution Substances 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 231100000004 severe toxicity Toxicity 0.000 description 1
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- 206010040872 skin infection Diseases 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 239000012899 standard injection Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 239000003206 sterilizing agent Substances 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000007916 tablet composition Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 201000008827 tuberculosis Diseases 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361775089P | 2013-03-08 | 2013-03-08 | |
| US61/775,089 | 2013-03-08 | ||
| PCT/US2014/021946 WO2014138639A1 (en) | 2013-03-08 | 2014-03-07 | Crystalline forms of d-glucitol, 1-deoxy-1-(methylamino)-, 1-(6-amino-3, 5-difluoropyridine-2-yl)-8-chloro-6-fluoro-1, 4-dihydro-7-(3-hydroxyazetidin-1-yl)-4-oxo-3-quinolinecarboxylate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2016511273A true JP2016511273A (ja) | 2016-04-14 |
Family
ID=51492015
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015561727A Pending JP2016511273A (ja) | 2013-03-08 | 2014-03-07 | D−グルシトール,1−デオキシ−1−(メチルアミノ)−,1−(6−アミノ−3,5−ジフルオロピリジン−2−イル)−8−クロロ−6−フルオロ−1,4−ジヒドロ−7−(3−ヒドロキシアゼチジン−1−イル)−4−オキソ−3−キノリンカルボン酸塩の結晶型 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20160046603A1 (es) |
| EP (1) | EP2964652A4 (es) |
| JP (1) | JP2016511273A (es) |
| CN (1) | CN105189513A (es) |
| AR (1) | AR095203A1 (es) |
| AU (1) | AU2014225392A1 (es) |
| BR (1) | BR112015021725A2 (es) |
| CA (1) | CA2903755A1 (es) |
| EA (1) | EA201591668A1 (es) |
| HK (1) | HK1219476A1 (es) |
| IL (1) | IL241045A0 (es) |
| MX (1) | MX2015011651A (es) |
| TW (1) | TW201514165A (es) |
| WO (1) | WO2014138639A1 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105693695A (zh) * | 2014-11-24 | 2016-06-22 | 重庆医药工业研究院有限责任公司 | 一种德拉沙星葡甲胺盐的晶型及其制备方法 |
| CN105017223B (zh) * | 2015-07-08 | 2017-08-01 | 扬子江药业集团有限公司 | 德拉沙星葡甲胺晶型i及其制备方法 |
| CN105017224A (zh) * | 2015-07-10 | 2015-11-04 | 扬子江药业集团有限公司 | 一种德拉沙星葡甲胺晶型的制备方法 |
| CN106916142A (zh) * | 2015-12-25 | 2017-07-04 | 江苏奥赛康药业股份有限公司 | 一种制备高纯度德拉沙星的方法 |
| CN110467600A (zh) * | 2018-05-10 | 2019-11-19 | 上海度德医药科技有限公司 | 一种德拉沙星葡甲胺盐晶型l及其制备方法 |
| CN113018268B (zh) * | 2019-12-25 | 2024-02-02 | 鲁南制药集团股份有限公司 | 一种注射用德拉沙星葡甲胺冻干制剂及其制备方法 |
| WO2022240897A1 (en) * | 2021-05-10 | 2022-11-17 | Sepelo Therapeutics, Llc | Pharmaceutical composition comprising delafloxacin for administration into the lung |
| CN116514775B (zh) * | 2022-01-20 | 2024-11-29 | 安徽普利药业有限公司 | 一种徳拉沙星葡甲胺盐新晶型及其制备方法 |
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| JPS57134482A (en) * | 1981-02-13 | 1982-08-19 | Dainippon Pharmaceut Co Ltd | 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8- naphthyridine-3-carboxylic acid-3/2 hydrate and its preparation |
| SI3056492T1 (sl) * | 2004-10-08 | 2022-03-31 | Abbvie Inc. | Sol meglumina in njene kristalinične oblike zdravila (delafloksacin) |
| US20070238719A1 (en) * | 2005-05-10 | 2007-10-11 | Hopkins Scott J | Method for reducing the risk of or preventing infection due to surgical or invasive medical procedures |
| TW200744598A (en) * | 2005-09-28 | 2007-12-16 | Daiichi Seiyaku Co | Process for the production of freeze-dried preparations containing quinolones |
| WO2008085913A1 (en) * | 2007-01-04 | 2008-07-17 | Rib-X Pharmaceuticals, Inc. | Methods for treating, preventing, or reducing the risk of opthalmic, otic, and nasal infections |
| MY161597A (en) * | 2008-11-15 | 2017-04-28 | Rib-X Pharmaceuticals Inc | Antimicrobial compositions |
-
2014
- 2014-03-07 MX MX2015011651A patent/MX2015011651A/es unknown
- 2014-03-07 CA CA2903755A patent/CA2903755A1/en not_active Abandoned
- 2014-03-07 BR BR112015021725A patent/BR112015021725A2/pt not_active IP Right Cessation
- 2014-03-07 CN CN201480013112.9A patent/CN105189513A/zh active Pending
- 2014-03-07 WO PCT/US2014/021946 patent/WO2014138639A1/en not_active Ceased
- 2014-03-07 EP EP14760249.4A patent/EP2964652A4/en not_active Withdrawn
- 2014-03-07 HK HK16107424.3A patent/HK1219476A1/zh unknown
- 2014-03-07 AU AU2014225392A patent/AU2014225392A1/en not_active Abandoned
- 2014-03-07 EA EA201591668A patent/EA201591668A1/ru unknown
- 2014-03-07 US US14/773,655 patent/US20160046603A1/en not_active Abandoned
- 2014-03-07 JP JP2015561727A patent/JP2016511273A/ja active Pending
- 2014-03-10 AR ARP140100810A patent/AR095203A1/es unknown
- 2014-03-10 TW TW103108122A patent/TW201514165A/zh unknown
-
2015
- 2015-09-02 IL IL241045A patent/IL241045A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2964652A1 (en) | 2016-01-13 |
| AR095203A1 (es) | 2015-09-30 |
| BR112015021725A2 (pt) | 2017-07-18 |
| EP2964652A4 (en) | 2016-10-12 |
| CN105189513A (zh) | 2015-12-23 |
| EA201591668A1 (ru) | 2016-02-29 |
| WO2014138639A1 (en) | 2014-09-12 |
| AU2014225392A1 (en) | 2015-09-24 |
| HK1219476A1 (zh) | 2017-04-07 |
| TW201514165A (zh) | 2015-04-16 |
| CA2903755A1 (en) | 2014-09-12 |
| MX2015011651A (es) | 2016-08-08 |
| US20160046603A1 (en) | 2016-02-18 |
| IL241045A0 (en) | 2015-11-30 |
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